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Catalogus nummer: (APOSOR917582-5G)
Leverancier: Apollo Scientific
Omschrijving: N-Acetyl-DL-norleucine 95%
UOM: 1 * 5 g


Catalogus nummer: (TCIAA2652-1G)
Leverancier: TCI
Omschrijving: Nε-acetyl-L-lysine ≥98.0% (by titrimetric analysis)
UOM: 1 * 1 g


Catalogus nummer: (TCIAA0125-25G)
Leverancier: TCI
Omschrijving: N-Acetyl-DL-valine ≥98.0% (by titrimetric analysis)
UOM: 1 * 25 g


Leverancier: Apollo Scientific
Omschrijving: 1-Acetyl-5-amino-2,3-dihydro-(1H)-indole, Technical Grade

Catalogus nummer: (APOSOR913438-1G)
Leverancier: Apollo Scientific
Omschrijving: (2-Acetyl-phenoxy)-acetic acid 95%
UOM: 1 * 1 g


Catalogus nummer: (APOSOR32514-1G)
Leverancier: Apollo Scientific
Omschrijving: 1-Acetyl-N-(3-ethynylphenyl)piperidine-4-carboxamide, tech
UOM: 1 * 1 g


Leverancier: TCI
Omschrijving: N-Acetyl-L-glutamic acid ≥98.0% (by HPLC, titration analysis)

Catalogus nummer: (PRSI91-248)
Leverancier: ProSci Inc.
Omschrijving: Uroporphyrinogen-III Synthase is an enzyme which belongs to the uroporphyrinogen-III synthase family. Uroporphyrinogen-III Synthase is ubiquitous and it is involved in Porphyrin metabolism. Porphyrins act as cofactors for a multitude of enzymes that perform a variety of processes within the cell such as Methionine synthesis (Vitamin B12) or oxygen transport (Heme). Uroporphyrinogen-III Synthase can catalyze cyclization of the linear Tetrapyrrole, Hydroxymethylbilane, to the Macrocyclic Uroporphyrinogen III, the branch point for the various sub-pathways leading to the wide diversity of Porphyrins. Defects in Uroporphyrinogen-III Synthase are the cause of Congenital Erythropoietic Porphyria (CEP).
UOM: 1 * 1 EA


Catalogus nummer: (PRSI92-113)
Leverancier: ProSci Inc.
Omschrijving: Cystathionine Gamma-Lyase (CTH) belongs to the trans-sulfuration enzymes family. CTH exists as a homotetramer and interacts with CALM in a calcium-dependent manner. CTH breaks down cystathionine into cysteine, ammonia and 2-oxobutanoate. CTH catalyses the last step in the trans-sulfuration pathway from methionine to cysteine and has broad substrate specificity. Defects in CTH will lead to cystathioninuria, which is an autosomal recessive phenotype characterised by abnormal accumulation of plasma cystathionine.
UOM: 1 * 1 EA


Leverancier: Apollo Scientific
Omschrijving: 3-Acetyl-2,5-dichlorothiophene

Catalogus nummer: (TCIAM2958-1G)
Leverancier: TCI
Omschrijving: 4-Acetyl-N-methylaniline ≥98.0% (by GC, titration analysis)
UOM: 1 * 1 g


Leverancier: TCI
Omschrijving: 1,2,3,4-Tetra-O-acetyl-ɑ-L-fucopyranose ≥98.0% (by HPLC)

Leverancier: Apollo Scientific
Omschrijving: Methyl 2,3,6,2',3',4',6'-hepta-O-acetyl-β-D-maltopyranoside ≥98%

Leverancier: TCI
Omschrijving: 9-Acetyl-3,6-diiodocarbazole ≥96.0% (by total nitrogen basis)

Catalogus nummer: (APOSOR346429-250MG)
Leverancier: Apollo Scientific
Omschrijving: 4-Acetyl-1H-pyrrole-2-carboxaldehyde ≥97%
UOM: 1 * 250 mg


Leverancier: Apollo Scientific
Omschrijving: 4-Methoxyphenyl 2,3,6-tri-O-acetyl-β-D-glucopyranoside ≥98%

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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
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